K242996
- 510(k) number
- K242996
- Device name
- EndyMed PRO MAX
- Applicant
- Endymed Medical, Ltd. IL
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-06-10
- Date received
- 2024-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K242996.pdf
Official FDA record: K242996
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.